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rs532190594

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs532190594(C;T)
Make rs532190594(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108140107
GeneACAT1
is asnp
is mentioned by
dbSNPrs532190594
dbSNP (old)rs532190594
ClinGenrs532190594
ebirs532190594
HLIrs532190594
Exacrs532190594
Gnomadrs532190594
Varsomers532190594
Maprs532190594
PheGenIrs532190594
Biobankrs532190594
1000 genomesrs532190594
hgdprs532190594
ensemblrs532190594
gopubmedrs532190594
geneviewrs532190594
scholarrs532190594
googlers532190594
pharmgkbrs532190594
gwascentralrs532190594
openSNPrs532190594
23andMers532190594
23andMe allrs532190594
SNP Nexus

SNPshotrs532190594
SNPdbers532190594
MSV3drs532190594
GWAS Ctlgrs532190594
Max Magnitude0
ClinVar
Risk rs532190594(T;T)
Alt rs532190594(T;T)
Reference Rs532190594(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ACAT1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.108010834C>T
CLNSRC
CLNACC RCV000434420.1,